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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440310Generated: October 24, 2026

Dicyclohexylcarbodiimide → HCID 15342494, compound

https://huagongshe.com/en/reaction/440310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantThieno[2,3-b]pyridin-3-amineHCID 289923—
SolventDichloromethaneHCID 6344—
ProductHCID 15342494HCID 1534249485.5%

Reaction Steps

1,3-Dicyclohexylcarbodiimide (11 g) was added with stirring to a solution of 3-aminothieno[2,3-b]pyridine (8 g) and N-(tert-butoxycarbonyl)glycine (10 g) in 200 mL of dichloromethane. After one hour the reaction mixture was filtered to remove the separated 1,3-dicyclohexylurea and evaporated to an oil. Crystallization from ethyl ether afforded 14 g of a solid, m.p. 190°-192° C. Recrystallization of 3 g from acetonitrile afforded 2.4 g of crystals, m.p. 192°-194° C. Final recrystallization from acetonitrile afforded 2.0 g of crystals, m.p. 194°-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519032
Source datasetuspto-grants-1996_05
ORD IDord-ce41ca38361d40198b362580e4dbc8b1
Source noteuspto-grants-1996_05