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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351263Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 131716169, compound

https://huagongshe.com/reaction/2351263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-HCID 85083—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ProductHCID 131716169HCID 131716169—

Reaction Steps

Using GlyOMe·HCl (30.2 g), Boc-Proline (4.3 g), HOBt (28.37 g) and WSCD (38.43 ml), the process was carried out similarly as in Example 16, whereby slightly yellowish oily product was obtained (BOc-Pro-GlyOMe). The product (10.31 g) in dioxane (5ml) was added to 4.32 N-HCl in dioxane (30 ml) in an ice bath, then stirred for 30 min. at room temperature. The solution was evaporated and dried in vacuo, thereafter dissolved in DMF (30 ml) and neutralized by addition of NMM (0.5 ml). Boc-Proline (6.46 g), HOBt (4.05 g) in DMF (30 ml) was treated with WSCD (5.49 ml) and stirred for 30 min. in an ice bath. The solution was added to above neutralized solution and stirred for 2 hrs. at 0° C. and further overnight at room temperature. The solution was evaporated and dissolved in CHCl3 (300 ml), then washed with 5 % aqueous sodium bicarbonate solution, 1N-HCl, 1N-NaOH in this order. The solution was dehydrated and concentrated to give an oily product (16.84 g) (Boc-Pro-Pro-GlyOMe). Rf=0.65 (CHCl3 :EtOH:AcOEt 5:2:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873087
Source datasetuspto-grants-1989_10
ORD IDord-c95355fbef8a4e729011c5d1b7f5dcb2
Source noteuspto-grants-1989_10