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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723189Generated: November 1, 2026

1,3-DI-Boc-2-methylisothiourea → HCID 178503639, compound

https://huagongshe.com/reaction/723189

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DI-Boc-2-methylisothioureaHCID 546603—
ReactantHCID 145857703HCID 145857703—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 178503639HCID 17850363968%

Reaction Steps

1,3-Bis-t-butoxycarbonyl-2-methyl-2-thiopseudourea (0.033 g, 0.114 mmol) was added to a solution of [(4-{4′-amino-6′-methyl-2′-[3-(2-phenylamino-ethyl)-ureido]-biphenyl-3-sulfonyl}-5-methylsulfanyl-thiophen-2-yl)-imino-methyl]-carbamic acid tert-butyl ester [example 216, step a] in methanol [1 mL] and 1 drop of acetic acid. The reaction was stirred at room temperature for 1 hour and evaporated. The reaction was evaporated and column chromatography (25% EtOAc in hexanes) of the residue yielded the title compound (0.072 g, 68%) as a solid. ESI-MS (m/z): Calcd. for C44H56N8O9S3: 936.33; found: 936.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138530B2
Source datasetuspto-grants-2006_11
ORD IDord-f748d7eb8be646dba85cacec50e2f11f
Source noteuspto-grants-2006_11