Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298635Generated: October 30, 2026

Thiourea → Isopropyl 4-(2-amino(1,3-thiazol-4-yl))-5-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/2298635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantIsopropyl 4-(2-bromoacetyl)-5-methylthiophene-2-carboxylateHCID 18537306—
ProductIsopropyl 4-(2-amino(1,3-thiazol-4-yl))-5-methylthiophene-2-carboxylateHCID 18536917107.1%

Reaction Steps

A solution of 260 mg (0.85 mmol) of isopropyl 4-(2-bromoacetyl)-5-methylthiophene-2-carboxylate was reacted with 65 mg (0.85 mmol) of thiourea in a manner similar to Example 8, step (a) to give isopropyl 4-(2-amino(1,3-thiazol-4-yl))-5-methylthiophene-2-carboxylate (257 mg, quantitive yield) as a white solid. 1H-NMR (DMSO-d6; 300 MHz) δ7.90 (s, 1H), 6.93 (s, 1H), 5.09 (septet, 1H, J=6.2 Hz), 2.61 (s, 3H), 1.29 (d, 6H, J=6.2 Hz). Mass spectrum (ESI, m/z): Calcd. for C12H14N2O2S2 283.1 (M+H), found 283.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-08a124dc255943bbb34f104e3816d056
Source noteuspto-grants-2002_12